Flecainide Acetate
- Product NDC
- 71335-2172
- 11-digit product format
- 713352172
- Labeler code
- 71335
- Product ID
- 71335-2172_d2b04520-2e5c-4986-949a-7ec3919022d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Flecainide Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202821
- Marketing category
- ANDA
- Marketing start
- 2015-07-08
- Substance
- FLECAINIDE ACETATE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| M8U465Q1WQ | FLECAINIDE ACETATE | 54143-56-5 | FLECAINIDE ACETATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2172-1 | 71335217201 | 30 TABLET in 1 BOTTLE (71335-2172-1) | 30 tablet | 2022-10-03 | No | No | Historical |
| 71335-2172-2 | 71335217202 | 90 TABLET in 1 BOTTLE (71335-2172-2) | 90 tablet | 2022-10-03 | No | No | Historical |
| 71335-2172-3 | 71335217203 | 60 TABLET in 1 BOTTLE (71335-2172-3) | 60 tablet | 2022-10-03 | No | No | Historical |
| 71335-2172-4 | 71335217204 | 180 TABLET in 1 BOTTLE (71335-2172-4) | 180 tablet | 2022-10-03 | No | No | Historical |